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使用多位点特异性寡核苷酸探针进行人类β-珠蛋白基因复合体的单倍型分析。

Haplotype analysis of the human beta-globin gene complex using multiple locus specific oligonucleotide probes.

作者信息

Nozari G, Rahbar S, Wallace R B

机构信息

City of Hope National Medical Center, Duarte, California 91010.

出版信息

Anal Biochem. 1988 Jul;172(1):180-4. doi: 10.1016/0003-2697(88)90429-0.

DOI:10.1016/0003-2697(88)90429-0
PMID:2903694
Abstract

Three oligonucleotide probes complementary to specific DNA sequences of the six human globin genes (epsilon, G gamma, A gamma, psi beta, delta, beta) were synthesized. The oligonucleotides were used either singly or in combination as hybridization probes to determine the haplotype of the human beta-globin gene cluster employing the four conventionally used restriction endonucleases HincII, HindIII, AvaII, and BamHI, in addition to HpaI. Polymorphism in the epsilon- and psi beta-genes (HincII) can be simultaneously determined with a single probe mixture. One of the probes complementary to both the psi beta- and gamma-genes is useful for determining both HindIII and HincII polymorphisms. The advantages of these probes relative to conventional cDNA probes are discussed.

摘要

合成了与六种人类珠蛋白基因(ε、Gγ、Aγ、ψβ、δ、β)的特定DNA序列互补的三种寡核苷酸探针。这些寡核苷酸单独或组合用作杂交探针,除了HpaI之外,还使用四种常规使用的限制性内切酶HincII、HindIII、AvaII和BamHI来确定人类β-珠蛋白基因簇的单倍型。ε-和ψβ-基因(HincII)中的多态性可以用单一探针混合物同时测定。与ψβ-和γ-基因都互补的一种探针可用于确定HindIII和HincII多态性。讨论了这些探针相对于传统cDNA探针的优势。

相似文献

1
Haplotype analysis of the human beta-globin gene complex using multiple locus specific oligonucleotide probes.使用多位点特异性寡核苷酸探针进行人类β-珠蛋白基因复合体的单倍型分析。
Anal Biochem. 1988 Jul;172(1):180-4. doi: 10.1016/0003-2697(88)90429-0.
2
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The rabbit alpha-like globin gene cluster is polymorphic both in the sizes of BamHI fragments and in the numbers of duplicated sets of genes.兔α-类珠蛋白基因簇在BamHI片段大小和基因重复序列数量上均具有多态性。
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Molecular cloning of human epsilon-globin gene.人类ε-珠蛋白基因的分子克隆
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Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules.通过单个DNA分子的酶促扩增解析的多个多态性单倍型。
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6296-300. doi: 10.1073/pnas.87.16.6296.